A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045745



Internal ID18788276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10765..60860hg38UCSC Ensembl
Innerchr16:60765..110858hg19UCSC Ensembl
Innerchr16:765..50858hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850096
hg1950094
hg1850094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2688n100
Supporting Variantsnssv3556924, nssv3556925, nssv3556926
Samples
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2, POLR3K, RHBDF1, SNRNP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045745
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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